Ibuprofen - 0363-0292-15 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 0363-0292
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 0363-0292
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 19880524

Package Information of Ibuprofen

Package NDC: 0363-0292-15
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0363-0292-15) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 0363-0292-15
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0363-0292-15) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 0363-0292
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19880524
Marketing Category Name ANDA
Labeler Name WALGREEN CO.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information